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Quotient Sciences
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Quotient Sciences is a drug development services provider, focused on helping our clients reduce the time and cost of bringing a drug to market.
Quotient Sciences is a drug development services provider, focused on helping our clients reduce the time and cost of bringing a drug to market.

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Scientific poster download - ‘Comparisons between US and UK Regulatory Environments for Conducting Phase I Clinical Research’

➡️ https://goo.gl/dpkvMg
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Learn how to save valuable API, through significant reductions in the amount of drug product manufactured.

Register for our upcoming webinar titled: 'Translational Pharmaceutics and the Benefits of Real-Time Adaptive Manufacturing'.

https://goo.gl/Nw7RB1

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Can I integrate CDMO & CRO services to accelerate my drug development?

Quotient is your answer.

Our Translational Pharmaceutics platform transforms the traditional approach of outsourcing development work to separate contract development and manufacturing organizations (CDMOs) and contract research organizations (CROs) – simplifying and streamlining your outsourcing and program management.

Learn more: https://goo.gl/NsRz1h
Translational Pharmaceutics
Translational Pharmaceutics
quotientsciences.com
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Our vision is to transform drug development with science and innovation by applying our quality, passion and expertise to accelerate the delivery of new medicines to patients.

Do you want to see science advanced so drug development becomes more efficient and new treatments reach patients faster?

Quotient is your answer.

Get in touch today: www.quotientsciences.com
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We've been very busy filling lots of roles here at Quotient Sciences but we still have a number of fantastic career opportunities available in Nottingham, Reading, Edinburgh, Miami and Philadelphia! If you are looking for your next move and would like to join a growing, stable and exciting company then take a look at our current vacancies and apply now! https://lnkd.in/gEHU2zg
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Partner with a dedicated project manager. We will execute your clinical pharmacology program on time and to the highest quality, providing customized service to speed your early drug development.

Contact us now: https://goo.gl/JsV75P
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Visit booth #19 at the upcoming DDF Summit in San Francisco
Nikki Whitfield, VP, CDMO Services, be delivering a presentation titled: 'How do I develop spray dried dispersions for early phase clinical trials and beyond?'. It will start at 11.20am on Monday, September 10.

The presentation will cover:

• Benefits of spray-drying to address poor drug solubility;
• Fit-for-purpose systems in early clinical research & effectively transitioning to solid oral dosage forms;
• Adaptive manufacturing “tailored” to the clinical study and patient recruitment.

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Celina Alvarez, our Executive Director of Project Management and Client Services, shares insights on how to recruit specialty volunteer populations for early phase clinical research - https://goo.gl/oRiCw1
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Leverage our proven track record in early phase. With experience of more than 1,300 Phase I studies, our experts secure the clinical pharmacology data you need to make critical program decisions.

Learn how: https://goo.gl/NQKJGC
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The HRA and MHRA have been exploring opportunities to improve the service being offered for the approval and ongoing management of Clinical Trials of Medicinal Products (CTIMPs) and launched a pilot to test an integrated process – the Combined Ways of Working Pilot.

Quotient Sciences is delighted to be taking part in the pilot and on Friday 22 June 2018 made its first two pilot Phase I submissions. This pilot process involved single applications submitted to both MHRA and Ethics and will help the authorities further develop and test their integrated review and approval process moving forward.

For more information, please click here: http://ow.ly/wiix30kGsT5
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